Evidence map›Paper›PMID 9037047›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

Triplet repeat polymorphism in the transmembrane region of the MICA gene: a strong association of six GCT repetitions with Behçet disease.

N Mizuki, M Ota, M Kimura, S Ohno, H Ando, Y Katsuyama, M Yamazaki, K Watanabe, K Goto, S Nakamura and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 5 pooled it
9.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

95 citing papers in PubMed, 5 syntheses or guidelines pooled it, 370 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Review
  8. Association ofZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Life (Basel, Switzerland) · 2022
    Article
  13. Genetics in Behcet's Disease: An Update Review.Frontiers in ophthalmology · 2022
    Review
  14. Review
  15. The Immunogenetics of Behcet's Disease.Advances in experimental medicine and biology · 2022
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Clinical and Genetic Aspects of Behçet's Disease in Japan.Internal medicine (Tokyo, Japan) · 2019
    Review

35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

N MizukiDepartment of Ophthalmology, Yokohama City University School of Medicine, Kanazawa-ku, Kanagawa, Japan.
M Ota
M Kimura
S Ohno
H Ando
Y Katsuyama
M Yamazaki
K Watanabe
K Goto
S Nakamura
S Bahram
H Inoko
Shinshu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A member of a novel family of the human major histocompatibility complex (MHC) class I genes termed MIC (MHC class I chain-related genes), MICA, has been recently identified near the HLA-B gene on the short arm of human chromosome 6. The predicted amino acid sequence of the MICA chain suggests that it folds similarly to typical class I chains and may have the capacity to bind peptides or other short ligands. Therefore, MICA is predicted to have a specialized function in antigen presentation or T cell recognition. During nucleotide sequence analyses of the MICA genomic clone, we found a triplet repeat microsatellite polymorphism of (GCT/AGC)n in the transmembrane (TM) region of the MICA gene. In 68 HLA homozygous B cell lines, 5 distinct alleles of this microsatellite sequence were detected. One of them contained an additional one base insertion that created a frameshift mutation resulting in a premature termination codon in the TM region. This particular allele may encode a soluble, secreted form of the MICA molecule. In addition, we have investigated this microsatellite polymorphism in 77 Japanese patients with Behcet disease, which is known to be associated with HLA-B51. The microsatellite allele consisting of 6 repetitions of GCT/AGC was present at significantly higher frequency in the patient group (Pc = 0.00055) than in a control population. Furthermore, the (GCT/AGC)6 allele was present in all B51 positive patients and in an additional 13 B51 negative patients. These results suggest the possibility of a primary association of Behcet disease with MICA rather than HLA-B.

Indexed as

Polymorphism, GeneticAsian PeopleBase SequenceBehcet SyndromeB-LymphocytesCell LineChi-Square DistributionChromosomes, Artificial, YeastChromosomes, Human, Pair 6CosmidsExonsFemaleHistocompatibility Antigens Class IHLA-B51 AntigenHLA-B AntigensHumansHistocompatibility Antigens Class IHLA-B51 AntigenHLA-B AntigensMembrane ProteinsMHC class I-related chain A

Identifiers

PMID9037047
PMCPMC19785
OpenAlexW1964922876

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.